| Title : An expeditious enantioselective total synthesis of valilactone - Wu_2006_J.Org.Chem_71_5748 |
| Author(s) : Wu Y , Sun YP |
| Ref : J Org Chem , 71 :5748 , 2006 |
|
Abstract :
The title compound was synthesized through an expeditious route using Crimmins aldolization to establish the two key stereogenic centers and a hydroxyl group activation (HGA) protocol to construct the anti alpha,beta-disubstituted beta-lactone from the corresponding syn aldol. |
| PubMedSearch : Wu_2006_J.Org.Chem_71_5748 |
| PubMedID: 16839158 |
| Inhibitor | Valilactone |
Wu Y, Sun YP (2006)
An expeditious enantioselective total synthesis of valilactone
J Org Chem
71 :5748
Wu Y, Sun YP (2006)
J Org Chem
71 :5748